Gene >> HOXA13
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222753 |
| Start |
27198245:27198245(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1120A>G |
| AA Mutation |
p.Arg374Gly(p.R374G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222753 |
| Start |
27199279:27199279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.799G>A |
| AA Mutation |
p.Glu267Lys(p.E267K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |